WO2008066704A3 - Procédé d'amélioration de la biodisponibilité pour les barbituriques non sédatifs - Google Patents

Procédé d'amélioration de la biodisponibilité pour les barbituriques non sédatifs Download PDF

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Publication number
WO2008066704A3
WO2008066704A3 PCT/US2007/023918 US2007023918W WO2008066704A3 WO 2008066704 A3 WO2008066704 A3 WO 2008066704A3 US 2007023918 W US2007023918 W US 2007023918W WO 2008066704 A3 WO2008066704 A3 WO 2008066704A3
Authority
WO
WIPO (PCT)
Prior art keywords
improving bioavailability
mmmdpb
dmmdpb
dpb
geometric mean
Prior art date
Application number
PCT/US2007/023918
Other languages
English (en)
Other versions
WO2008066704A2 (fr
Inventor
Avraham Yacobi
Daniel Aaron Moros
Derek Ganes
Original Assignee
Taro Pharmaceuticals Usa Inc
Avraham Yacobi
Daniel Aaron Moros
Derek Ganes
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Taro Pharmaceuticals Usa Inc, Avraham Yacobi, Daniel Aaron Moros, Derek Ganes filed Critical Taro Pharmaceuticals Usa Inc
Priority to EP07867444A priority Critical patent/EP2081576A4/fr
Publication of WO2008066704A2 publication Critical patent/WO2008066704A2/fr
Publication of WO2008066704A3 publication Critical patent/WO2008066704A3/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • A61K31/515Barbituric acids; Derivatives thereof, e.g. sodium pentobarbital
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs

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  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Psychology (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

L'administration d'acide 1,3-diméthoxyméthyl-5,5-diphénylbarbiturique et de ses composés apparentés avec des aliments augmente la biodisponibilité de ces composés. Les rapports (à la diète/nourri) pour la moyenne géométrique AUC0-t étaient de 35,6 % (DMMDPB), de 36,6 % (MMMDPB) et de 65,3 % (DPB) et pour la moyenne géométrique Cmax ils étaient de 14,6 % (DMMDPB), de 31,9 % (MMMDPB) et de 62,9 % (DPB). Les uréides cycliques peuvent être administrés à un sujet avant ou après ingestion d'aliment dans une période de temps définie.
PCT/US2007/023918 2006-11-14 2007-11-14 Procédé d'amélioration de la biodisponibilité pour les barbituriques non sédatifs WO2008066704A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP07867444A EP2081576A4 (fr) 2006-11-14 2007-11-14 Procédé d'amélioration de la biodisponibilité pour les barbituriques non sédatifs

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85870106P 2006-11-14 2006-11-14
US60/858,701 2006-11-14

Publications (2)

Publication Number Publication Date
WO2008066704A2 WO2008066704A2 (fr) 2008-06-05
WO2008066704A3 true WO2008066704A3 (fr) 2009-04-02

Family

ID=39468451

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2007/023918 WO2008066704A2 (fr) 2006-11-14 2007-11-14 Procédé d'amélioration de la biodisponibilité pour les barbituriques non sédatifs

Country Status (3)

Country Link
US (1) US20080132529A1 (fr)
EP (1) EP2081576A4 (fr)
WO (1) WO2008066704A2 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6756379B2 (en) * 2001-07-26 2004-06-29 Taro Pharmaceutical Industries Ltd. Non-sedating barbiturate compounds as neuroprotective agents
CL2003002588A1 (es) * 2002-12-11 2005-01-07 Taro Pharmaceuticals Ireland L Uso de una composicion farmaceutica que comprende acido n,n-dimetoximetildifenil barbiturico, acido n-metoximetildifenil barbiturico o acido difenil barbiturico o una sal farmaceuticamente aceptable del mismo para preparar un medicamento util en el t
CN105250316B (zh) * 2015-11-14 2018-01-19 西安力邦制药有限公司 一种含二联苯酚的抗癫痫药物组合

Citations (3)

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Publication number Priority date Publication date Assignee Title
US4628056A (en) * 1983-09-14 1986-12-09 Taro Pharmaceutical Industries Ltd. Novel oxopyrimidine derivatives, pharmaceutical compositions containing them and their use as anticonvulsant, antianxiety and muscle relaxant agents
US6756379B2 (en) * 2001-07-26 2004-06-29 Taro Pharmaceutical Industries Ltd. Non-sedating barbiturate compounds as neuroprotective agents
US6939873B2 (en) * 2000-07-26 2005-09-06 Taro Pharmaceuticals Industries Limited Non-sedating barbituric acid derivatives

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US3919427A (en) * 1972-06-02 1975-11-11 Kendall & Co Therapeutic compositions containing 1-methyl-3-alkoxymethyl-5,5-disubstituted barbituric acid compounds
US3904627A (en) * 1972-06-02 1975-09-09 Kendall & Co 1-methyl-3-alkoxymethyl-5,5-disubstituted barbituric acid compounds
US3900475A (en) * 1972-06-26 1975-08-19 Kendall & Co Certain phenobarbital salts
US3948896A (en) * 1973-02-28 1976-04-06 The Kendall Company N-mono(alkoxymethyl) phenobarbitals, process therefor and therapeutic composition and method containing same
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DE3374684D1 (en) * 1982-08-31 1988-01-07 Daikin Ind Ltd A method to trap the enolate ion of the malonic acid or its derivatives
IT1196500B (it) * 1986-07-16 1988-11-16 Eniricerche Spa Derivati dell'acido malonico e metodi per la loro sintesi
HU196775B (en) * 1986-08-05 1989-01-30 Richter Gedeon Vegyeszet Process for production of morfologically unique new modifications of famotidin and medical compositions containing such substances
US4833148A (en) * 1987-04-09 1989-05-23 Washington University Method of using alkenyl- or alkynyl-substituted thiobarbiturates to reduce neurotoxic injury
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US5456851A (en) * 1994-04-07 1995-10-10 Johnson & Johnson Consumer Products, Inc. Ketoconazole shampoo containing butylated hydroxytoluene or butylated hydroxyanisole
RU2147584C1 (ru) * 1995-10-27 2000-04-20 Американ Цианамид Компани Способ получения дигалоидазолопиримидинов и способ получения дигидроксиазолопиримидинов
KR100194535B1 (ko) * 1995-12-27 1999-06-15 우종일 아릴 벤조일 우레아 유도체 및 이를 함유하는 농약조성물
WO1998029408A1 (fr) * 1996-12-26 1998-07-09 Nikken Chemicals Co., Ltd. Derives de n-hydroxyuree et compositions medicinales a base de ces derives
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EP1051181B1 (fr) * 1997-12-31 2004-03-17 The University Of Kansas Remedes contenant des precurseurs hydrosolubles d'amines tertiaires, et leurs procedes d'obtention
DE69906960T2 (de) * 1998-05-08 2004-01-29 Smithkline Beecham Plc Phenylurea und phenylthio urea derivate
US6156925A (en) * 1998-09-25 2000-12-05 American Cyanamid Company Process for the preparation of halogenated phenylmaloates
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Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4628056A (en) * 1983-09-14 1986-12-09 Taro Pharmaceutical Industries Ltd. Novel oxopyrimidine derivatives, pharmaceutical compositions containing them and their use as anticonvulsant, antianxiety and muscle relaxant agents
US6939873B2 (en) * 2000-07-26 2005-09-06 Taro Pharmaceuticals Industries Limited Non-sedating barbituric acid derivatives
US6756379B2 (en) * 2001-07-26 2004-06-29 Taro Pharmaceutical Industries Ltd. Non-sedating barbiturate compounds as neuroprotective agents

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2081576A4 *

Also Published As

Publication number Publication date
EP2081576A2 (fr) 2009-07-29
WO2008066704A2 (fr) 2008-06-05
US20080132529A1 (en) 2008-06-05
EP2081576A4 (fr) 2010-06-30

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